chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	149382373	149382374	T	C	21	GENIC	homozygous	111772204
3	149382614	149382615	G	C	24	GENIC	homozygous	111772206
3	149384015	149384016	T	C	28	GENIC	homozygous	111772208
3	149384789	149384790	C	T	16	GENIC	homozygous	111772210
3	149384795	149384796	A	G	19	GENIC	homozygous	111772212
3	149385451	149385452	C	T	26	GENIC	homozygous	111772218
3	149385864	149385865	C	T	17	GENIC	homozygous	111772220
3	149387268	149387269	G	A	28	GENIC	homozygous	111772222
3	149388883	149388884	G	A	39	GENIC	possibly homozygous	111772224
3	149388909	149388910	A	G	40	GENIC	possibly homozygous	111772226
3	149390713	149390714	G	T	22	GENIC	possibly homozygous	111772228
3	149390868	149390869	T	G	21	GENIC	homozygous	111772230
3	149391316	149391317	T	A	28	GENIC	possibly homozygous	111772232
3	149391588	149391589	G	A	27	GENIC	homozygous	111772234
3	149391914	149391915	C	A	35	GENIC	homozygous	111772236
3	149392638	149392639	T	C	19	GENIC	homozygous	111772238
3	149392877	149392878	T	C	32	GENIC	homozygous	111772240
3	149393287	149393288	T	G	34	GENIC	homozygous	111772242
3	149393497	149393498	G	A	32	GENIC	homozygous	111772244
3	149393525	149393526	A	C	31	GENIC	homozygous	111772246
3	149393717	149393718	A	G	23	GENIC	homozygous	111772248